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510(k) K831686

CHLAMYDIA OVERBY MEDIA by Viromed Laboratories, Inc. — Product Code KIT

K831686 is an FDA 510(k) premarket notification submitted by Viromed Laboratories, Inc. for the device "CHLAMYDIA OVERBY MEDIA". The FDA issued a decision of Substantially Equivalent on July 7, 1983. The device falls under product code KIT (Media And Components, Synthetic Cell And Tissue Culture), a Class I device regulated under 21 CFR 864.2220. Viromed Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 7, 1983
Date Received
May 24, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Media And Components, Synthetic Cell And Tissue Culture
Device Class
Class I
Regulation Number
864.2220
Review Panel
PA
Submission Type

Other clearances by Viromed Laboratories, Inc.

  • K951440 — LLC-MK2 (MONKEY KIDNEY, MACACA MULATA) CELL CULTURE (May 22, 1996)
  • K951461 — NCI-H292 CELL CULTURE (May 22, 1996)
  • K871613 — BUFFALO GREEN MONKEY KIDNEY CELLS (May 13, 1987)
  • K862555 — HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA) (July 10, 1986)
  • K861373 — HUMAN LUNG CARCINOMA CELLS (A549) (April 18, 1986)
  • K853695 — RESPIRATORY SYNCYTIAL VIRUS ID REAGENT (December 4, 1985)
  • K852396 — HEK (July 12, 1985)
  • K852395 — MINK LUNG (July 12, 1985)
  • K852394 — MDCK (July 12, 1985)
  • K843252 — AFRICAN GREEN SV 5/SV 40 (September 6, 1984)

Other clearances for product code KIT

  • K892938 — AMNIO-GROW TM (May 22, 1989)
  • K890700 — MELANOCYTE GROWTH MEDIUM (MGM) (February 24, 1989)
  • K890701 — ENDOTHELIAL GROWTH MEDIUM (EGM) (February 24, 1989)
  • K890482 — ABC, ABC-1X, ABC(TM) (February 10, 1989)
  • K884654 — ALPHACALF SERUM (November 30, 1988)
  • K884574 — DME & HAM'S NUTRIENT MIXTURE, PROD. NO. D9785 (November 22, 1988)
  • K884573 — HBSS W/O CALC CHLOR/MAG SULF/PHEN RED/SB NO. H4891 (November 22, 1988)
  • K884572 — RPMI-1640 HYBRI-MAX, PROD. NO. R5382 (November 22, 1988)
  • K883065 — ALLOPREP SYSTEM (October 13, 1988)
  • K884031 — FBS, EQ., OR FETAL BOVINE SERUM EQUIVALENT (October 6, 1988)

FDA data resources